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Searched for days. Results 1061 to 1070 of 1865 total matches.
Once-a-week Alendronate (Fosamax)
The Medical Letter on Drugs and Therapeutics • Mar 19, 2001 (Issue 1100)
mg daily 54.73
treatment
* Cost for 28 days’ treatment based on AWP listings in Drug Topics Red ...
Once-a-week formulations of alendronate (Fosamax) in 35- and 70-mg tablets have now been approved by the FDA and are being heavily promoted for prevention and treatment of postmenopausal osteoporosis. A new formulation of risedronate (Actonel) for once-a-week use is under development and may be available next year.
What Comes After Metformin for Type 2 Diabetes?
The Medical Letter on Drugs and Therapeutics • Jul 23, 2012 (Issue 1395)
. Approximate cost of 30 days’ treatment. Based on wholesale acquisition cost (WAC). Source: PricePointRx ...
Most experts agree that lifestyle modifications and
metformin (Glucophage, and others) should be used
first to treat patients with type 2 diabetes. If metformin
alone fails to control hyperglycemia, there is
no general agreement on which drug should be
added next. A recent article in The Medical Letter
offered some support for a sulfonylurea. Three
recent trials published in The Lancet favored the
long-acting basal insulin glargine, the glucagon-like
peptide (GLP-1) analog exenatide, and the dipeptidyl
peptidase-4 (DPP-4) inhibitor linagliptin, respectively.
Some of the advantages...
An OTC Corticosteroid Nasal Spray for Allergic Rhinitis
The Medical Letter on Drugs and Therapeutics • Nov 11, 2013 (Issue 1429)
may not be achieved for 7-
14 days. In patients with seasonal allergic rhinitis,
intranasal corticosteroid sprays ...
The FDA has approved the over-the-counter (OTC)
sale of Nasacort Allergy 24HR (Sanofi), a triamcinolone
acetonide nasal spray previously available only
by prescription as Nasacort AQ. The OTC product,
which is scheduled to be marketed in the spring of
2014, will be the first corticosteroid nasal spray that
can be purchased without a prescription in the US.
Nasacort Allergy 24HR is approved for use in patients
≥2 years old with nasal allergy symptoms.
Ibrutinib (Imbruvica) for Chronic Lymphocytic Leukemia
The Medical Letter on Drugs and Therapeutics • Apr 14, 2014 (Issue 1440)
be reduced to 140
mg/day. The cost for 30 days’ treatment with ibrutinib for
CLL is $8200.9
CONCLUSION ...
The FDA has approved ibrutinib (eye broo' ti nib;
Imbruvica – Janssen/Pharmacyclics), an oral kinase
inhibitor, for second-line treatment of chronic
lymphocytic leukemia (CLL). It is the first kinase inhibitor
to be approved for CLL. Ibrutinib was approved earlier
for second-line treatment of mantle cell lymphoma, a
rare form of B-cell non-Hodgkins lymphoma.
Dichlorphenamide (Keveyis) for Periodic Paralysis
The Medical Letter on Drugs and Therapeutics • Apr 11, 2016 (Issue 1492)
levels should be
measured periodically. The cost of a 30-day supply
of Keveyis (50 mg twice daily ...
Dichlorphenamide (Keveyis – Taro), an oral carbonic
anhydrase inhibitor, has been approved by the
FDA for treatment of primary hypokalemic and
hyperkalemic periodic paralysis and related variants.
Dichlorphenamide is the first drug to be approved in
the US for this indication. It was approved as Daranide
in 1958 for treatment of glaucoma, but had not been
marketed since 2002.
Pimavanserin (Nuplazid) for Parkinson's Disease Psychosis
The Medical Letter on Drugs and Therapeutics • Jun 06, 2016 (Issue 1496)
per day. If a strong CYP3A4 inducer must be
used, an increase in the dose of pimavanserin ...
The FDA has approved the atypical antipsychotic
pimavanserin (Nuplazid – Acadia) for treatment
of hallucinations and delusions associated with
Parkinson's disease. It is the first drug to be approved
in the US for this indication.
In Brief: Olmesartan and Sprue-Like Enteropathy
The Medical Letter on Drugs and Therapeutics • Jan 29, 2018 (Issue 1539)
for the
first 56 days of neratinib treatment. The labeling
specifies a number of dosage adjustments that should ...
A reader asked whether healthcare providers should avoid prescribing the angiotensin receptor blocker (ARB) olmesartan medoxomil (Benicar, and others) because it can cause severe GI adverse effects.In 2013, the FDA warned that olmesartan can cause sprue-like enteropathy, a condition characterized by intestinal villous atrophy, severe chronic diarrhea, and significant unintended weight loss. The warning was based on 23 cases of serious sprue-like enteropathy associated with use of olmesartan, some occurring years after starting the drug. All patients improved after stopping olmesartan; 10 had a...
Neratinib (Nerlynx) for HER2-Positive Breast Cancer
The Medical Letter on Drugs and Therapeutics • Jan 29, 2018 (Issue 1539)
for the
first 56 days of neratinib treatment. The labeling
specifies a number of dosage adjustments that should ...
The FDA has approved the oral tyrosine kinase
inhibitor neratinib (Nerlynx – Puma Biotechnology)
for extended adjuvant treatment of adults with early-stage,
human epidermal growth factor receptor 2
(HER2)-positive breast cancer, following adjuvant
trastuzumab (Herceptin)-based therapy. HER2 is
overexpressed in about 20% of breast cancers. Up
to 30% of early-stage, HER2-positive breast cancer
cases treated with trastuzumab-based adjuvant
therapy recur.
Apalutamide (Erleada) for Prostate Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jul 16, 2018 (Issue 1551)
in
the apalutamide group had a seizure 354 to 475 days
after starting treatment; no seizures occurred ...
Apalutamide (Erleada – Janssen) has received
accelerated approval from the FDA for treatment of
nonmetastatic castration-resistant prostate cancer.
It is the first drug to be approved in the US for this
indication. Apalutamide is an oral antiandrogen that
binds to the ligand-binding domain of the androgen
receptor.
Niraparib/Abiraterone Acetate (Akeega) for Prostate Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023 (Issue 1684)
receive a GnRH
analog concurrently or should have had a bilateral
orchiectomy. A 30-day supply of Zejula ...
Akeega (Janssen), a fixed-dose combination of
the oral poly(ADP-ribose) polymerase (PARP)
inhibitor niraparib (Zejula) and the antiandrogen
abiraterone acetate (Zytiga, and others), has been
approved by the FDA for use in combination with
prednisone for treatment of adults with deleterious
or suspected deleterious BRCA-mutated (BRCAm)
metastatic castration-resistant prostate cancer
(mCRPC). Niraparib has been available since 2017
for treatment of epithelial ovarian, fallopian tube, or
primary peritoneal cancer. Abiraterone acetate has
been available since 2011 for treatment of CRPC...
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e146-7 doi:10.58347/tml.2023.1684c | Show Introduction Hide Introduction